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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430403Generated: October 26, 2026

Benzyl Alcohol → 5-benzyloxy-N-methyl-2-nitroaniline

https://huagongshe.com/reaction/1430403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantMethylamineHCID 6329—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-DifluoronitrobenzeneHCID 67967—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5-benzyloxy-N-methyl-2-nitroanilineHCID 6795405196%

Reaction Conditions

Temperature37.5 °C

Reaction Steps

An aqueous solution of 40% methyl amine (8.2 mL, 94.2 mmol) was added dropwise to a toluene solution (50 mL) of 2,4-difluoronitrobenzene (5.0 g, 31.4 mmol) under ice cooling, and the mixture was stirred at 35-40° C. for 2 hours. Water was added to the reaction solution, and toluene extraction was performed, followed by washing with water. Benzyl alcohol (6.5 mL, 62.8 mmol), tetrabutyl ammonium bromide (1.0 g, 3.1 mmol) and potassium carbonate (5.2 g, 37.6 mmol) were added to the resulting organic layer, and the mixture was heated under reflux for 4 hours. After the reaction solution was cooled, water (25 mL) was added, and the mixture was stirred at 70° C. for 1 hour. The mixture was stirred under ice cooling for 30 minutes, and precipitated crystals were collected by filtration. The resulting crystals were washed with water and dried at 50° C., thereby obtaining 7.8 g of orange, powdery 5-benzyloxy-N-methyl-2-nitroaniline (yield: 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940889B2
Source datasetuspto-grants-2015_01
ORD IDord-806c977f8adb4f3a86a7056da02ed655
Source noteuspto-grants-2015_01